Medable Agent Studio is a no-code, AI-powered platform designed for sponsors and clinical research organizations (CROs) to build, deploy, and scale custom or pre-built agents that automate and optimize clinical trial workflows. The platform enables teams to quickly configure agents for tasks such as protocol development, trial planning, and monitoring, removing bottlenecks and reducing unproductive "white space" between trial phases. Agent Studio integrates seamlessly with over 13 clinical and enterprise systems, supports regulatory and validation requirements (GxP, ICH, HIPAA, GDPR, CDISC), and maintains human-in-the-loop oversight for transparency and control. The platform includes ready-to-go agents like the CRA Agent, which aggregates and summarizes data across systems, automates routine monitoring, and empowers clinical research associates to focus on data quality and patient safety.

## Key Features

No-Code Agent Builder Enables rapid creation and deployment of custom or pre-built AI agents for clinical workflows.

• No programming required; clinical teams configure agents directly
• Supports bespoke and ready-to-go agent builds

System Integration Connects with 13+ clinical and enterprise platforms for unified data flow.

• Integrates with eCOA, Veeva EDC, IRT, CTMS, Salesforce, Microsoft, Gmail
• Eliminates manual data stitching and silos

Regulatory Compliance Built to meet life sciences standards and regulatory requirements.

• Supports GxP, ICH, HIPAA, GDPR, CDISC
• Incorporates SOPs, validation, and benchmarking

Human-in-the-Loop Oversight Allows teams to set automation guardrails and maintain control.

• Aligns agent actions with team workflows
• Ensures transparency and safety in critical processes

CRA Agent (Clinical Research Associate Agent) Pre-built agent for monitoring and data aggregation.

• Surfaces insights and risks from multiple systems
• Automates routine monitoring and communication tasks

## Benefits

Accelerated Clinical Trial Timelines Reduces delays and unproductive time between trial phases.

• Automates manual work and removes bottlenecks
• Enables faster study startup and execution

Operational Efficiency Streamlines workflows and reduces tech burden for clinical teams.

• Frees staff from repetitive tasks
• Empowers focus on data quality, patient safety, and site relationships

Compliance and Transparency Ensures regulatory adherence and oversight.

• Human-in-the-loop controls for critical safety and compliance
• Benchmarking against trusted industry sources

Scalability and Flexibility Supports both ready-to-go and custom agent builds for diverse needs.

• Adapts to specific trial requirements and organizational workflows
• Scales across sponsors, CROs, and global studies